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Featured researches published by E. Gardner.


Human Genetics | 1994

A multiple interval physical map of the pericentromeric region of human chromosome 10

Alan Tunnacliffe; Michael S. Jackson; E. Gardner; Donald R. Love; Julie Moore; S. E. Mole; Lois M. Mulligan; A. Graham; G. Finocchiaro; S. Ørstavik; Bruce A.J. Ponder

Five intervals in the pericentromeric region of human chromosome 10 have been defined using a panel of somatic cell hybrids carrying portions of the chromosome. The map positions of twelve markers, consisting of four genes and eight anonymous DNA segments, have been localized by assignment to one of the five intervals. Several other markers could be placed in specific intervals by genetic linkage to assigned loci. When previously published data are incorporated, the summary map of the pericentromeric region encompasses thirty-two loci in bands 10p11.2-q11.2.


Genomics | 1992

Complementary physical and genetic techniques map the vinculin (VCL) gene on chromosome 10q

Lois M. Mulligan; E. Gardner; Håkan Telenius; Bruce A.J. Ponder

Vinculin is a cytoskeletal protein component of adherens type cell junctions. The gene had been mapped to 10q11.2-qter. We have used a combination of physical and genetic mapping techniques to refine this localization. Hybridization of the vinculin cDNA probe, HV1, to a human-rodent somatic hybrid panel initially suggested a position of either 10q11.2 or 10q22.1-10q23. Genetic recombination mapping in three-generation families with multiple endocrine neoplasia type 2 (MEN2) indicated a position distal to D10S22 (10q21.1) in 10q22.1-10q23. This was confirmed by hybridization of the vinculin cDNA to flow-sorted translocation derivative chromosomes containing the q21-qter portion of chromosome 10. We conclude that the vinculin locus maps in 10q22.1-q23, distal to D10S22.


Nature | 1993

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A

Lois M. Mulligan; John B. Kwok; Catherine S. Healey; Mark J. Elsdon; Charis Eng; E. Gardner; Donald R. Love; Sara E. Mole; Julie Moore; Laura Papi; Margaret A. Ponder; Håkan Telenius; Alan Tunnacliffe; Bruce A.J. Ponder


Nature Genetics | 1994

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

Lois M. Mulligan; Charis Eng; Catherine S. Healey; David G. Clayton; John B. Kwok; E. Gardner; Margaret A. Ponder; Andrea Frilling; Charles E. Jackson; Hendrik Lehnert; Hartmut P. H. Neumann; Stephen N. Thibodeau; Bruce A.J. Ponder


Human Molecular Genetics | 1994

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

Charis Eng; Darrin P. Smith; Lois M. Mulligan; Maria A. Nagal; Catherine S. Healey; Margaret A. Ponder; E. Gardner; G. F. W. Scheumann; CharIes E. Jackson; Alan Tunnacllffe; Bruce A.J. Ponder


Genes, Chromosomes and Cancer | 1993

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

Lois M. Mulligan; E. Gardner; Barbara A. Smith; Chris Mathew; Bruce A.J. Ponder


Human Molecular Genetics | 1993

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.

E. Gardner; Laura Papi; Douglas F. Easton; Tim Cummings; Charles E. Jackson; Michael M. Kaplan; Donald R. Love; Sara E. Mole; Julie Moore; Lois M. Mulligan; Robert A. Norum; Margaret A. Ponder; Seymour Reichlin; Glenn Stall; Håkan Telenius; Margareta Telenius-Berg; Alan Tunnacliffe; Bruce A.J. Ponder


Oncogene | 1993

Structural analysis of the human ret proto-oncogene using exon trapping

John B. Kwok; E. Gardner; J. P. Warner; Bruce A.J. Ponder; Lois M. Mulligan


Human Molecular Genetics | 1994

Haplotype analysis of MEN 2 mutations

E. Gardner; Lois M. Mulligan; Charis Eng; Catherine S. Healey; John B. Kwok; Margaret A. Ponder; Bruce A.J. Ponder


Human Molecular Genetics | 1993

A polymorphic dinucleotide repeat at the ZNF22 locus

Donald R. Love; E. Gardner; Bruce A.J. Ponder

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